510(k) K980556

LIQUICHEK CARDIAC MARKERS CONTROL LT by Bio-Rad — Product Code JJT

K980556 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "LIQUICHEK CARDIAC MARKERS CONTROL LT". The FDA issued a decision of Substantially Equivalent on February 25, 1998. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 25, 1998
Date Received
February 13, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Controls (Assayed And Unassayed)
Device Class
Class I
Regulation Number
862.1660
Review Panel
CH
Submission Type